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HRID 2410294作成日:2026年10月27日

Dimethylformamide → 1-(4-Chloro-2-nitrophenyl)piperidine

https://huagongshe.com/reaction/2410294

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物2,5-DichloronitrobenzeneHCID 6977—
反応物PiperidineHCID 8082—
溶媒WaterHCID 962—
生成物1-(4-Chloro-2-nitrophenyl)piperidineHCID 28531896.4%

反応手順

Piperidine (660 μl, 6.66 mmol, commercially available product) was added at room temperature to an N,N-dimethylformamide (DMF; 1 ml) solution of 1,4-dichloro-2-nitrobenzene (390 mg, 2.03 mmol, commercially available product). The resulting mixture was stirred for 18.5 hours. Water was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30 g, hexane/ethyl acetate=10/1). Thus, 1-(4-chloro-2-nitrophenyl)piperidine (471 mg, 96.4%) was yielded as an orange-colored oily material.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08816089B2
出典データセットuspto-grants-2014_08
ORD IDord-ee91ea45b0904751abc05dcff34d888c
出典メモuspto-grants-2014_08